Tulogdi Aron, Biro Laszlo, Barsvari Beata, Stankovic Mona, Haller Jozsef, Toth Mate
Institute of Experimental Medicine, Department of Behavioral Neuroscience, P.O. Box 67, H-1450 Budapest, Hungary.
Institute of Experimental Medicine, Department of Behavioral Neuroscience, P.O. Box 67, H-1450 Budapest, Hungary.
Behav Brain Res. 2015 Apr 15;283:108-15. doi: 10.1016/j.bbr.2015.01.030. Epub 2015 Jan 28.
Our recent studies showed that brain areas that are activated in a model of escalated aggression overlap with those that promote predatory aggression in cats. This finding raised the interesting possibility that the brain mechanisms that control certain types of abnormal aggression include those involved in predation. However, the mechanisms of predatory aggression are poorly known in rats, a species that is in many respects different from cats. To get more insights into such mechanisms, here we studied the brain activation patterns associated with spontaneous muricide in rats. Subjects not exposed to mice, and those which did not show muricide were used as controls. We found that muricide increased the activation of the central and basolateral amygdala, and lateral hypothalamus as compared to both controls; in addition, a ventral shift in periaqueductal gray activation was observed. Interestingly, these are the brain regions from where predatory aggression can be elicited, or enhanced by electrical stimulation in cats. The analysis of more than 10 other brain regions showed that brain areas that inhibited (or were neutral to) cat predatory aggression were not affected by muricide. Brain activation patterns partly overlapped with those seen earlier in the cockroach hunting model of rat predatory aggression, and were highly similar with those observed in the glucocorticoid dysfunction model of escalated aggression. These findings show that the brain mechanisms underlying predation are evolutionarily conservative, and indirectly support our earlier assumption regarding the involvement of predation-related brain mechanisms in certain forms of escalated social aggression in rats.
我们最近的研究表明,在升级攻击模型中被激活的脑区与促进猫的掠食性攻击的脑区重叠。这一发现提出了一个有趣的可能性,即控制某些类型异常攻击的脑机制包括那些参与捕食的机制。然而,掠食性攻击的机制在大鼠中却鲜为人知,大鼠在许多方面与猫不同。为了更深入地了解这些机制,我们在此研究了与大鼠自发杀鼠行为相关的脑激活模式。未接触过小鼠的动物以及未表现出杀鼠行为的动物被用作对照。我们发现,与两个对照组相比,杀鼠行为增加了中央杏仁核、基底外侧杏仁核和下丘脑外侧的激活;此外,还观察到导水管周围灰质激活的腹侧移位。有趣的是,这些正是在猫中通过电刺激可引发或增强掠食性攻击的脑区。对其他10多个脑区的分析表明,抑制(或对)猫的掠食性攻击无影响的脑区不受杀鼠行为的影响。脑激活模式部分与大鼠掠食性攻击的蟑螂捕食模型中早期观察到的模式重叠,并且与在升级攻击的糖皮质激素功能障碍模型中观察到的模式高度相似。这些发现表明,捕食背后的脑机制在进化上是保守的,并间接支持了我们早期关于与捕食相关的脑机制参与大鼠某些形式的升级社会攻击的假设。